Clinical Database and Biobank of Patients With Gynecologic Neoplasms (NCT01267851) | Clinical Trial Compass
UnknownNot Applicable
Clinical Database and Biobank of Patients With Gynecologic Neoplasms
China1,600,000 participantsStarted 2010-01-01
Plain-language summary
The database and biobank establishment started in 1997 in our institute. However, the sample size was too small with respect to our clinical and fundamental scientific research's requirement. Thus the Chinese gynecological oncology study (GOS) group was established to create a large multicentre database and biobank of patients with gynecologic diseases.
Who can participate
Age range
18 Years – 75 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* patients with informed consent;
* patients with gynecologic diseases;
* patients with intact clinical and pathological information
Exclusion Criteria:
* not included in the inclusion criteria
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial is described as a clinical database and biobank — does that mean it only involves collecting my medical records and tissue samples, or would it require any additional procedures or treatments beyond my standard care?
2Since this study covers several different gynecologic conditions including my specific diagnosis, can you explain how my data and biological samples would actually be used, and who would have access to them?
3The recruitment status for this study is listed as unknown — is this study still actively enrolling patients at this institution, and if so, is now a good time for me to consider joining?
4Would participating in this biobank study in any way affect or delay the treatment plan you're recommending for me, or does it run completely alongside my normal care?
5Are there any privacy or long-term implications I should think about before agreeing to have my medical information and tissue samples stored in a research database, and how long would they be kept?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Trial details
NCT IDNCT01267851
SponsorHuazhong University of Science and Technology